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Your search keyword '"Chenevix-Trench, G"' showing total 27 results

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27 results on '"Chenevix-Trench, G"'

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1. Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum.

2. Understanding the genetic complexity of puberty timing across the allele frequency spectrum.

3. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses.

4. Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes.

5. A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer.

6. Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.

7. Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes.

8. Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk.

9. Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.

10. Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.

11. Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer.

12. Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair.

13. Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer.

14. Identification of six new susceptibility loci for invasive epithelial ovarian cancer.

15. A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia.

16. Large-scale genotyping identifies 41 new loci associated with breast cancer risk.

17. Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer.

18. Genome-wide association studies identify four ER negative-specific breast cancer risk loci.

19. GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.

20. Genome-wide association analysis identifies three new breast cancer susceptibility loci.

21. A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population.

22. Common variants at 19p13 are associated with susceptibility to ovarian cancer.

23. A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24.

24. A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2.

25. Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.

26. A common coding variant in CASP8 is associated with breast cancer risk.

27. Atopy in Australia.

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